FDA 510(k) Applications Submitted by DIANA L WOLANIUK

FDA 510(k) Number Submission Date Device Name Applicant
K060964 04/07/2006 ARCHITECT BNP ASSAY, MODEL 8K28 FUJIREBIO DIAGNOSTICS, INC.
K052000 07/25/2005 ARCHITECT CA 19-9XR ASSAY FUJIREBIO DIAGNOSTICS, INC.
K052889 10/13/2005 VITROS CA 19-9 FUJIREBIO DIAGNOSTICS, INC.


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